NM_001099922.3(ALG13):c.2606C>T (p.Ala869Val) AND Developmental and epileptic encephalopathy, 36
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001081591.9
Allele description [Variation Report for NM_001099922.3(ALG13):c.2606C>T (p.Ala869Val)]
NM_001099922.3(ALG13):c.2606C>T (p.Ala869Val)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024